Deficient Muscle Carnitine Transport in Primary Carnitine Deficiency-Reference-Cited by-同舟云学术

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Deficient Muscle Carnitine Transport in Primary Carnitine Deficiency

Published:1997-11 Issue:5 Volume:42 Page:583-587
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Pons Roser,Carrozzo Rosalba,Tein Ingrid,Walker Winsome F,Addonizio Linda J,Rhead William,Miranda Armand F,Dimauro Salvatore,De Vivo Darryl C

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference28 articles.

1. Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts

2. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

3. Impaired Skin Fibroblast Carnitine Uptake in Primary Systemic Carnitine Deficiency Manifested by Childhood Carnitine-Responsive Cardiomyopathy

4. Carnitine deficiency presenting as familial cardiomyopathy: A treatable defect in carnitine transport

Cited by 38 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis;Clinica Chimica Acta;2020-06

2. Carnitine deficiency: Risk factors and incidence in children with epilepsy;Brain and Development;2015-09

3. Lipid Storage Myopathies Due to Fatty Acid Oxidation Defects;Neuromuscular Disorders of Infancy, Childhood, and Adolescence;2015

4. Metabolic Myopathies;Neuromuscular Disorders in Clinical Practice;2013-04-26

5. Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1;Analytical and Bioanalytical Chemistry;2012-11-10

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